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Human Genetics|October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderJillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.Nature Genetics|February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsVivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.Nature Genetics|February 27, 2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Peter Szatmari, Andrew D Paterson, et al.Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.Nature Genetics|March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusionsWouter De Coster, Marleen Van den Broeck, Matt Baker, et al.Molecular Psychiatry|December 5, 2024
X-chromosome-wide association study for Alzheimer's diseaseJulie Le Borgne, Lissette Gomez, Sami Heikkinen, et al.Neurology|January 18, 2019
Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based settingGanesh Chauhan, Hieab H H Adams, Claudia L Satizabal, et al.Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.Nature Genetics|April 5, 2011
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's diseaseAdam C Naj, Gyungah Jun, Gary W Beecham, et al.Pageof 30